Objective: To examine empirical data on children with autistic disorde
r (AD), Asperger's disorder, and pervasive developmental disorder not
otherwise specified (PDD-NOS) for continuities or distinguishing featu
res between disorders and to see to what extent the Diagnostic and Sta
tistical Manual of Mental Disorders (DSM-IV) diagnostic criteria refle
ct observed data. Method: Studies were identified in 4 ways. 1) A Medl
ine search from 1976 to the present of articles with the key words aut
ism, pervasive developmental disorder, autistic spectrum disorder, and
Asperger, of these articles, those with mesh headings or textwords ''
cluster,'' which identified cluster analyses deriving pervasive develo
pmental disorder (PDD) subtypes, were retained. 2) The Journal of Auti
stic and Developmental Disorders from 1990 to the present was hand-sea
rched to identify other empirically derived studies on diagnosis, prev
alence, classification and validity of PDD subtypes. 3) Key review art
icles were searched for their references. 4) The references of all ide
ntified articles were searched. Results: Eight cluster studies were re
tained for their relevance to diagnostic issues, as were 7 empirically
derived studies delineating clinical characteristics of children with
AD, Asperger's syndrome, or PDD-NOS. Data suggest that children with
PDD may fit into 1 of 2 overlapping groups, including a lower-function
ing group with greater developmental compromise, social aloofness, and
a greater number of autistic symptoms and a higher-functioning group
with higher IQ, fewer autistic symptoms, and more prosocial behaviour.
The PDD subtypes resemble each other and can be seen as existing on a
continuum, differing only by degree of impairment. Conclusion: Childr
en exhibiting the triad of autistic impairments can be seen as sufferi
ng from disorders on a PDD continuum. While the DSM-IV does identify a
lower-functioning autistic group (AD), the higher-functioning group i
s less well sewed. Asperger's disorder as defined in the DSM-IV is not
clearly distinguishable from AD and PDD-NOS, and the PDD-NOS subcateg
ory is not operationalized. Further research is required to elaborate
criteria for the higher-functioning PDD group, and measures related to
etiology, outcome, and treatment response may help determine which di
agnostic criteria can meaningfully separate one disorder from another.